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Topical Vitamin D uses – Review March 2014


Topical in VitaminDWiki


Off-label uses of topical vitamin d in dermatology: a systematic review - 2014

J Cutan Med Surg. 2014 Mar 1;18(2):91-108.
Wat H, Dytoc M.

Background:Topical vitamin D is approved by the US Food and Drug Administration for the treatment of psoriasis but is also used off-label in the treatment of a variety of cutaneous diseases despite a lack of evidence-based guidelines.

Objective:The objective of this study was to provide evidence-based clinical guidelines for the off-label use of topical vitamin D in the treatment of dermatologic disease.Methods:A systematic literature review was conducted via the MEDLINE, Embase, and CENTRAL databases for off-label uses of topical vitamin D analogues in the treatment of dermatologic disease other than psoriasis. The data were synthesized, and evidence-based recommendations were rendered according to the highest level of evidence available.

Results:A total of 165 articles met the inclusion criteria.
A moderate to strong recommendation was given for the use of

  • topical vitamin D in combination with corticosteroids and phototherapy in vitiligo and as
  • monotherapy for various
    ichthyoses, [dry, scaling skin that may be thickened or very thin]
    morphea, [ isolated patches of hardened skin]
    pityriasis alba, [dry, fine-scaled, pale patches on the face]
    prurigo nodularis, [(itchy) nodules which usually appear on the arms or legs] and
    polymorphous light eruption. [itchy rash caused by sun exposure in people who have developed a sensitivity to sunlight]

There is evidence showing that topical vitamin D is ineffective in the treatment of

  • actinic keratosis,
  • seborrheic keratosis, [premalignant condition of thick, scaly, or crusty patches of skin.]
  • lichen planus,
  • seborrheic dermatitis,
  • alopecia areata, c
  • hemotherapy-induced alopecia, and
  • hypertrophic scars.

Conclusion:Topical vitamin D analogues have an important role in the off-label treatment of dermatologic disease, but higher quality studies are still required.


Topical 5,000 IU raised blood levels to 37 ng - RCT Oct 2018

Topical vitamin D3: A randomized controlled trial (RCT)
Clin Nutr ESPEN. 2018 Oct;27:16-19. doi: 10.1016/j.clnesp.2018.05.009. Epub 2018 Jun 28. PMID: 24636434
Topical vitamin D3: A randomized controlled trial (RCT).
Bubshait DA1, Al-Dakheel DA2, Alanii FM2.

  • 1 Department of Orthopaedic Surgery, College of Medicine, Imam AbdulRahman Bin Faisal University, Dammam; King Fahd Hospital of the University, Al Khobar, Saudi Arabia. Electronic address: dbubshait at iau.edu.sa.
  • 2 Department of Orthopaedic Surgery, College of Medicine, Imam AbdulRahman Bin Faisal University, Dammam; King Fahd Hospital of the University, Al Khobar, Saudi Arabia.

Note: For some people the vitamin D levels were DECREASED
Note: Vitamin D levels can be decreased for oral Vitamin D supplementation as well for some people
Image
OBJECTIVE: The intent of this study was to test the effect of Top-D, a topical Vitamin D preparation, in delivering vitamin D.

METHODS:
Five hundred and fifty healthy patients, with vitamin D insufficiency and deficiency were recruited after written informed consent. Demographic data was recorded, adequate history and clinical examination was done to rule out any metabolic diseases. Complete blood picture, serum calcium, phosphorous, Parathormone and 25 Hydroxy-vitamin D3 (25OHD) was carried out before enrollment of the patients. Patients were divided randomly into two groups 350 in study group and 200 in the control group. Patients in the study group were given Top-D (Vitamin D3 gel made from proniosomal technology) to apply daily on the skin. Top-D 1 g contained 5000 IU of vitamin D3. The control group was given 1 g of Aloe vera gel to be applied every day. The two groups had no knowledge to which group they belong. After 4 months serum 25OHD was tested again.

RESULTS: Three hundred and forty five patients in study group and 192 in control group completed the study. The mean age of the patients in the both the groups was 42 years (18-80 years). The pretreatment 25OHD level in the study group was 11.03 ± 4.57 (2-12) ng/l compared to the control group 10.36 ± 4.09 (2-21) and post treatment the levels were 37.17 ± 6.04 (12-54) ng/ml and 10.51 ± 3.5 (2-19) ng/ml (p < 0.001).

CONCLUSION: The results of this study indicate that transdermal route of vitamin D is potentially, safe and can give desired results to raise the vitamin D levels. This route is an alternate route for supplementation of vitamin D which should be utilized.

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Topical Vitamin D uses – Review March 2014        

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